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Analysis of circular genome rearrangement by fusions, fissions and block-interchanges

BACKGROUND: Analysis of genomes evolving via block-interchange events leads to a combinatorial problem of sorting by block-interchanges, which has been studied recently to evaluate the evolutionary relationship in distance between two biological species since block-interchange can be considered as a...

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Autores principales: Lu, Chin Lung, Huang, Yen Lin, Wang, Tsui Ching, Chiu, Hsien-Tai
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1569878/
https://www.ncbi.nlm.nih.gov/pubmed/16768797
http://dx.doi.org/10.1186/1471-2105-7-295
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author Lu, Chin Lung
Huang, Yen Lin
Wang, Tsui Ching
Chiu, Hsien-Tai
author_facet Lu, Chin Lung
Huang, Yen Lin
Wang, Tsui Ching
Chiu, Hsien-Tai
author_sort Lu, Chin Lung
collection PubMed
description BACKGROUND: Analysis of genomes evolving via block-interchange events leads to a combinatorial problem of sorting by block-interchanges, which has been studied recently to evaluate the evolutionary relationship in distance between two biological species since block-interchange can be considered as a generalization of transposition. However, for genomes consisting of multiple chromosomes, their evolutionary history should also include events of chromosome fusions and fissions, where fusion merges two chromosomes into one and fission splits a chromosome into two. RESULTS: In this paper, we study the problem of genome rearrangement between two genomes of circular and multiple chromosomes by considering fusion, fission and block-interchange events altogether. By use of permutation groups in algebra, we propose an [Formula: see text] (n(2)) time algorithm to efficiently compute and obtain a minimum series of fusions, fissions and block-interchanges required to transform one circular multi-chromosomal genome into another, where n is the number of genes shared by the two studied genomes. In addition, we have implemented this algorithm as a web server, called FFBI, and have also applied it to analyzing by gene orders the whole genomes of three human Vibrio pathogens, each with multiple and circular chromosomes, to infer their evolutionary relationships. Consequently, our experimental results coincide well with our previous results obtained using the chromosome-by-chromosome comparisons by landmark orders between any two Vibrio chromosomal sequences as well as using the traditional comparative analysis of 16S rRNA sequences. CONCLUSION: FFBI is a useful tool for the bioinformatics analysis of circular and multiple genome rearrangement by fusions, fissions and block-interchanges.
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spelling pubmed-15698782006-09-26 Analysis of circular genome rearrangement by fusions, fissions and block-interchanges Lu, Chin Lung Huang, Yen Lin Wang, Tsui Ching Chiu, Hsien-Tai BMC Bioinformatics Research Article BACKGROUND: Analysis of genomes evolving via block-interchange events leads to a combinatorial problem of sorting by block-interchanges, which has been studied recently to evaluate the evolutionary relationship in distance between two biological species since block-interchange can be considered as a generalization of transposition. However, for genomes consisting of multiple chromosomes, their evolutionary history should also include events of chromosome fusions and fissions, where fusion merges two chromosomes into one and fission splits a chromosome into two. RESULTS: In this paper, we study the problem of genome rearrangement between two genomes of circular and multiple chromosomes by considering fusion, fission and block-interchange events altogether. By use of permutation groups in algebra, we propose an [Formula: see text] (n(2)) time algorithm to efficiently compute and obtain a minimum series of fusions, fissions and block-interchanges required to transform one circular multi-chromosomal genome into another, where n is the number of genes shared by the two studied genomes. In addition, we have implemented this algorithm as a web server, called FFBI, and have also applied it to analyzing by gene orders the whole genomes of three human Vibrio pathogens, each with multiple and circular chromosomes, to infer their evolutionary relationships. Consequently, our experimental results coincide well with our previous results obtained using the chromosome-by-chromosome comparisons by landmark orders between any two Vibrio chromosomal sequences as well as using the traditional comparative analysis of 16S rRNA sequences. CONCLUSION: FFBI is a useful tool for the bioinformatics analysis of circular and multiple genome rearrangement by fusions, fissions and block-interchanges. BioMed Central 2006-06-12 /pmc/articles/PMC1569878/ /pubmed/16768797 http://dx.doi.org/10.1186/1471-2105-7-295 Text en Copyright © 2006 Lu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lu, Chin Lung
Huang, Yen Lin
Wang, Tsui Ching
Chiu, Hsien-Tai
Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title_full Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title_fullStr Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title_full_unstemmed Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title_short Analysis of circular genome rearrangement by fusions, fissions and block-interchanges
title_sort analysis of circular genome rearrangement by fusions, fissions and block-interchanges
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1569878/
https://www.ncbi.nlm.nih.gov/pubmed/16768797
http://dx.doi.org/10.1186/1471-2105-7-295
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